Suppr超能文献

性别和年龄对Wistar大鼠慢性炎症性疼痛的发生、维持及缓解的影响。

Sex and age effects on chronic inflammatory pain development, maintenance, and resolution in Wistar rats.

作者信息

Jones Andrea F, Wang Queenie, Rodríguez-Graciani Keishla M, Díaz Zaidmara T, Simon Liz, Gilpin Nicholas W

机构信息

Department of Physiology, Louisiana State University Health Sciences Center, New Orleans, LA 70112, United States; Southeast Louisiana VA Healthcare System, New Orleans, LA, United States.

Department of Physiology, Louisiana State University Health Sciences Center, New Orleans, LA 70112, United States; Southeast Louisiana VA Healthcare System, New Orleans, LA, United States.

出版信息

J Pain. 2025 Mar;28:104789. doi: 10.1016/j.jpain.2025.104789. Epub 2025 Jan 20.

Abstract

Millions of Americans live with chronic inflammatory pain conditions, and the prevalence of these conditions increases with age and is higher in females. Still, it is poorly understood how sex, age and peripheral gene expression affect the trajectory of chronic inflammatory pain conditions. We used the inflammatory agent, Complete Freund's Adjuvant (CFA), to systematically test sex and age effects on mechanical and thermal sensitivity in adolescent and adult male and female Wistar rats over 3 weeks (Experiment 1 [onset]) or 11 weeks (Experiment 2 [recovery]). We report that relative to male CFA rats, CFA females are mechanically hypersensitive at all time points and thermally hypersensitive at later time points (long-term during maintenance and recovery). Also, within CFA rats, more adult males (90%) achieved behavioral recovery at 11 weeks, relative to adolescent males (70%), adult females (70%) and adolescent females (50%). Behavioral recovery was most highly correlated with thermal nociception scores in most groups. Among adult males, significant positive correlations were seen between mechanical and thermal nociception scores and between scores in the CFA-injected and non-injected paws. In paw tissue from a subset of rats from experiment 2, we also report increased transient receptor potential cation channel subfamily V member 1 (TRPV1) gene expression in adult CFA but not adolescent CFA rats, and increased pro- and anti-inflammatory, and triglyceride synthesis-related gene expression in all CFA rats. Our results demonstrate apparent sex and age differences in the trajectory of chronic inflammatory pain-related behavior and gene expression in the affected paw of rats. PERSPECTIVE: This article highlights sex and age differences in the trajectory of chronic inflammatory pain and possible peripheral mechanisms driving recovery in Wistar rats. This data could be used to better understand recovery patterns in patients with this type of pain and provides a starting point for assessment of novel treatments.

摘要

数以百万计的美国人患有慢性炎症性疼痛疾病,这些疾病的患病率随年龄增长而增加,且女性患病率更高。然而,关于性别、年龄和外周基因表达如何影响慢性炎症性疼痛疾病的发展轨迹,我们仍知之甚少。我们使用炎性介质完全弗氏佐剂(CFA),在3周(实验1[发病期])或11周(实验2[恢复期])内,系统地测试了青春期和成年雄性及雌性Wistar大鼠的性别和年龄对机械敏感性和热敏感性的影响。我们发现,相对于雄性CFA大鼠,CFA雌性大鼠在所有时间点均表现出机械性超敏反应,在后期时间点(维持期和恢复期的长期阶段)表现出热超敏反应。此外,在CFA大鼠中,相对于青春期雄性大鼠(70%)、成年雌性大鼠(70%)和青春期雌性大鼠(50%),更多的成年雄性大鼠(90%)在11周时实现了行为恢复。在大多数组中,行为恢复与热痛觉评分的相关性最高。在成年雄性大鼠中,机械性和热痛觉评分之间以及注射CFA和未注射CFA的爪子的评分之间存在显著的正相关。在实验2的一部分大鼠的爪子组织中,我们还发现成年CFA大鼠而非青春期CFA大鼠的瞬时受体电位阳离子通道亚家族V成员1(TRPV1)基因表达增加,并且所有CFA大鼠的促炎、抗炎和甘油三酯合成相关基因表达均增加。我们的结果表明大鼠患侧爪子慢性炎症性疼痛相关行为和基因表达的发展轨迹存在明显的性别和年龄差异。观点:本文强调了Wistar大鼠慢性炎症性疼痛发展轨迹中的性别和年龄差异以及驱动恢复的可能外周机制。这些数据可用于更好地理解此类疼痛患者的恢复模式,并为评估新型治疗方法提供一个起点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验